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- B0ecb71a84394d83f217dc9f14a5e827c hasDbXref "Orphanet:1547" @default.
- B0ecb71a84394d83f217dc9f14a5e827c type Axiom @default.
- B0ecb71a84394d83f217dc9f14a5e827c annotatedProperty IAO_0000115 @default.
- B0ecb71a84394d83f217dc9f14a5e827c annotatedSource MONDO_0007409 @default.
- B0ecb71a84394d83f217dc9f14a5e827c annotatedTarget "Cryptomicrotia - brachydactyly - excess fingertip arch syndrome describes a combination of malformations that include bilateral cryptomicrotia, brachytelomesophalangy with short middle and distal phalanges of digits 2 through 5, hypoplastic toenails and excess fingertip arch patterns, and has been reported in one family (mother and son). Cryptomicrotia - brachydactyly - excess fingertip arch syndrome is thought to follow an autosomal dominant transmission. There have been no further descriptions in the literature since 1988." @default.